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I love that idea!!!!

mom of Makenzie 7 w/o cf and Jaelyn 2 w/ cf

A request.. FOR EVERYONE

Everyone,

can I have come up with this idea, and I want to run it by you

guys. I want to start a book, like a scrap book of CF kids, teens,

young adults and adults, and their families all around the world. A

book that will contain pictures, messages, whatever you'd like to place

in it, that would be sent from home to home where information about

that person and their family would be added.

I would start it, and with the permission of the people that sent me

pictures, I would place them in the book. Then I would send it to the

first person on the list, and on it would go. There is enough people

on this list alone to make for an interesting book, but then it could

go to others. Hopefully making it back to Canada so that I could see

it once in a while. It would join a community of people that is

relatively small, but that I think needs to stick together. Who knows,

it could be published one day. I think it would be amazing.

I would set it up that the person that got the book would email me and

I would direct where it would go next. (so personal information would

not be in the book and that mailing costs would be minimal/local) That

way we could keep track of it and keep in going all over. Imagine

sitting at home with your family and looking at picture after picture

of CF people all around the world. And reading their messages, hearing

what they have to say, hearing their story. I think it could be

beautiful, and with good organization and preparation, it could go on

and on and on. Imagine the possibilities. We could take it to

clinics, to have people join in. Each person that has it that moment

could get involved in any way that they like, perhaps collecting some

pictures and pasting them in yourself. It would give us all a week or

two of crafty fun, before mailing the book to its next temporary home.

Think about it everyone. This would be entirely your call whether to

participate, so if its not your thing, you could just take a look and

not put in pictures or messages. But for those that want to get really

involved it would be a beautiful way to join with the entire world of

CF families. I am going to start with my clinic, and my old kids

clinic. and with permission with the pictures that you guys sent me.

Which will be many already, and then send it to one of you to start the

chain. The possibilities of this amaze me, I think it could be magical.

Let me know what you guys think.

Natalia

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS.

------------------------------------

_____

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natalia i think it is a really cool idea and i would love to be a part of

it just let me know

michelle

mom t 4 girls the youngest w/cf (anna) A request.. FOR EVERYONE

> Everyone,

>

> can I have come up with this idea, and I want to run it by you

> guys. I want to start a book, like a scrap book of CF kids, teens,

> young adults and adults, and their families all around the world. A

> book that will contain pictures, messages, whatever you'd like to place

> in it, that would be sent from home to home where information about

> that person and their family would be added.

> I would start it, and with the permission of the people that sent me

> pictures, I would place them in the book. Then I would send it to the

> first person on the list, and on it would go. There is enough people

> on this list alone to make for an interesting book, but then it could

> go to others. Hopefully making it back to Canada so that I could see

> it once in a while. It would join a community of people that is

> relatively small, but that I think needs to stick together. Who knows,

> it could be published one day. I think it would be amazing.

>

> I would set it up that the person that got the book would email me and

> I would direct where it would go next. (so personal information would

> not be in the book and that mailing costs would be minimal/local) That

> way we could keep track of it and keep in going all over. Imagine

> sitting at home with your family and looking at picture after picture

> of CF people all around the world. And reading their messages, hearing

> what they have to say, hearing their story. I think it could be

> beautiful, and with good organization and preparation, it could go on

> and on and on. Imagine the possibilities. We could take it to

> clinics, to have people join in. Each person that has it that moment

> could get involved in any way that they like, perhaps collecting some

> pictures and pasting them in yourself. It would give us all a week or

> two of crafty fun, before mailing the book to its next temporary home.

>

> Think about it everyone. This would be entirely your call whether to

> participate, so if its not your thing, you could just take a look and

> not put in pictures or messages. But for those that want to get really

> involved it would be a beautiful way to join with the entire world of

> CF families. I am going to start with my clinic, and my old kids

> clinic. and with permission with the pictures that you guys sent me.

> Which will be many already, and then send it to one of you to start the

> chain. The possibilities of this amaze me, I think it could be magical.

>

> Let me know what you guys think.

>

> Natalia

>

>

> -------------------------------------------

> The opinions and information exchanged on this list should IN NO WAY

> be construed as medical advice.

>

> PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

>

> ------------------------------------

>

>

>

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YES, It would be just that MAGICAL>Great idea.

Love & hugs, grandmoMBEv

A request.. FOR EVERYONE

Everyone,

can I have come up with this idea, and I want to run it by you

guys. I want to start a book, like a scrap book of CF kids, teens,

young adults and adults, and their families all around the world. A

book that will contain pictures, messages, whatever you'd like to place

in it, that would be sent from home to home where information about

that person and their family would be added.

I would start it, and with the permission of the people that sent me

pictures, I would place them in the book. Then I would send it to the

first person on the list, and on it would go. There is enough people

on this list alone to make for an interesting book, but then it could

go to others. Hopefully making it back to Canada so that I could see

it once in a while. It would join a community of people that is

relatively small, but that I think needs to stick together. Who knows,

it could be published one day. I think it would be amazing.

I would set it up that the person that got the book would email me and

I would direct where it would go next. (so personal information would

not be in the book and that mailing costs would be minimal/local) That

way we could keep track of it and keep in going all over. Imagine

sitting at home with your family and looking at picture after picture

of CF people all around the world. And reading their messages, hearing

what they have to say, hearing their story. I think it could be

beautiful, and with good organization and preparation, it could go on

and on and on. Imagine the possibilities. We could take it to

clinics, to have people join in. Each person that has it that moment

could get involved in any way that they like, perhaps collecting some

pictures and pasting them in yourself. It would give us all a week or

two of crafty fun, before mailing the book to its next temporary home.

Think about it everyone. This would be entirely your call whether to

participate, so if its not your thing, you could just take a look and

not put in pictures or messages. But for those that want to get really

involved it would be a beautiful way to join with the entire world of

CF families. I am going to start with my clinic, and my old kids

clinic. and with permission with the pictures that you guys sent me.

Which will be many already, and then send it to one of you to start the

chain. The possibilities of this amaze me, I think it could be magical.

Let me know what you guys think.

Natalia

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

------------------------------------

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Thats a great idea...id love to be a part!Patty H

> Everyone,

>

> can I have come up with this idea, and I want to run it by you

> guys. I want to start a book, like a scrap book of CF kids, teens,

> young adults and adults, and their families all around the world.

A

> book that will contain pictures, messages, whatever you'd like to

place

> in it, that would be sent from home to home where information about

> that person and their family would be added.

> I would start it, and with the permission of the people that sent

me

> pictures, I would place them in the book. Then I would send it to

the

> first person on the list, and on it would go. There is enough

people

> on this list alone to make for an interesting book, but then it

could

> go to others. Hopefully making it back to Canada so that I could

see

> it once in a while. It would join a community of people that is

> relatively small, but that I think needs to stick together. Who

knows,

> it could be published one day. I think it would be amazing.

>

> I would set it up that the person that got the book would email me

and

> I would direct where it would go next. (so personal information

would

> not be in the book and that mailing costs would be minimal/local)

That

> way we could keep track of it and keep in going all over. Imagine

> sitting at home with your family and looking at picture after

picture

> of CF people all around the world. And reading their messages,

hearing

> what they have to say, hearing their story. I think it could be

> beautiful, and with good organization and preparation, it could go

on

> and on and on. Imagine the possibilities. We could take it to

> clinics, to have people join in. Each person that has it that

moment

> could get involved in any way that they like, perhaps collecting

some

> pictures and pasting them in yourself. It would give us all a week

or

> two of crafty fun, before mailing the book to its next temporary

home.

>

> Think about it everyone. This would be entirely your call whether

to

> participate, so if its not your thing, you could just take a look

and

> not put in pictures or messages. But for those that want to get

really

> involved it would be a beautiful way to join with the entire world

of

> CF families. I am going to start with my clinic, and my old kids

> clinic. and with permission with the pictures that you guys sent

me.

> Which will be many already, and then send it to one of you to start

the

> chain. The possibilities of this amaze me, I think it could be

magical.

>

> Let me know what you guys think.

>

> Natalia

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Everyone,

can I have come up with this idea, and I want to run it by you

guys. I want to start a book, like a scrap book of CF kids, teens,

young adults and adults, and their families all around the world. A

book that will contain pictures, messages, whatever you'd like to place

in it, that would be sent from home to home where information about

that person and their family would be added.

I would start it, and with the permission of the people that sent me

pictures, I would place them in the book. Then I would send it to the

first person on the list, and on it would go. There is enough people

on this list alone to make for an interesting book, but then it could

go to others. Hopefully making it back to Canada so that I could see

it once in a while. It would join a community of people that is

relatively small, but that I think needs to stick together. Who knows,

it could be published one day. I think it would be amazing.

I would set it up that the person that got the book would email me and

I would direct where it would go next. (so personal information would

not be in the book and that mailing costs would be minimal/local) That

way we could keep track of it and keep in going all over. Imagine

sitting at home with your family and looking at picture after picture

of CF people all around the world. And reading their messages, hearing

what they have to say, hearing their story. I think it could be

beautiful, and with good organization and preparation, it could go on

and on and on. Imagine the possibilities. We could take it to

clinics, to have people join in. Each person that has it that moment

could get involved in any way that they like, perhaps collecting some

pictures and pasting them in yourself. It would give us all a week or

two of crafty fun, before mailing the book to its next temporary home.

Think about it everyone. This would be entirely your call whether to

participate, so if its not your thing, you could just take a look and

not put in pictures or messages. But for those that want to get really

involved it would be a beautiful way to join with the entire world of

CF families. I am going to start with my clinic, and my old kids

clinic. and with permission with the pictures that you guys sent me.

Which will be many already, and then send it to one of you to start the

chain. The possibilities of this amaze me, I think it could be magical.

Let me know what you guys think.

Natalia

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Natalia,

I think that is a great idea! How cool to be able to look at the pics and read

the stories of so many others with CF!

A request.. FOR EVERYONE

Everyone,

can I have come up with this idea, and I want to run it by you

guys. I want to start a book, like a scrap book of CF kids, teens,

young adults and adults, and their families all around the world. A

book that will contain pictures, messages, whatever you'd like to place

in it, that would be sent from home to home where information about

that person and their family would be added.

I would start it, and with the permission of the people that sent me

pictures, I would place them in the book. Then I would send it to the

first person on the list, and on it would go. There is enough people

on this list alone to make for an interesting book, but then it could

go to others. Hopefully making it back to Canada so that I could see

it once in a while. It would join a community of people that is

relatively small, but that I think needs to stick together. Who knows,

it could be published one day. I think it would be amazing.

I would set it up that the person that got the book would email me and

I would direct where it would go next. (so personal information would

not be in the book and that mailing costs would be minimal/local) That

way we could keep track of it and keep in going all over. Imagine

sitting at home with your family and looking at picture after picture

of CF people all around the world. And reading their messages, hearing

what they have to say, hearing their story. I think it could be

beautiful, and with good organization and preparation, it could go on

and on and on. Imagine the possibilities. We could take it to

clinics, to have people join in. Each person that has it that moment

could get involved in any way that they like, perhaps collecting some

pictures and pasting them in yourself. It would give us all a week or

two of crafty fun, before mailing the book to its next temporary home.

Think about it everyone. This would be entirely your call whether to

participate, so if its not your thing, you could just take a look and

not put in pictures or messages. But for those that want to get really

involved it would be a beautiful way to join with the entire world of

CF families. I am going to start with my clinic, and my old kids

clinic. and with permission with the pictures that you guys sent me.

Which will be many already, and then send it to one of you to start the

chain. The possibilities of this amaze me, I think it could be magical.

Let me know what you guys think.

Natalia

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS.

------------------------------------

------------------------------------------------------------------------------

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I'd like my daughter to be a part of it. Definitely count us in.

Elias- dad to Uriah 4, no CF, Soley 1, w/CF

Re: A request.. FOR EVERYONE

Thats a great idea...id love to be a part!Patty H

> Everyone,

>

> can I have come up with this idea, and I want to run it by you

> guys. I want to start a book, like a scrap book of CF kids, teens,

> young adults and adults, and their families all around the world.

A

> book that will contain pictures, messages, whatever you'd like to

place

> in it, that would be sent from home to home where information about

> that person and their family would be added.

> I would start it, and with the permission of the people that sent

me

> pictures, I would place them in the book. Then I would send it to

the

> first person on the list, and on it would go. There is enough

people

> on this list alone to make for an interesting book, but then it

could

> go to others. Hopefully making it back to Canada so that I could

see

> it once in a while. It would join a community of people that is

> relatively small, but that I think needs to stick together. Who

knows,

> it could be published one day. I think it would be amazing.

>

> I would set it up that the person that got the book would email me

and

> I would direct where it would go next. (so personal information

would

> not be in the book and that mailing costs would be minimal/local)

That

> way we could keep track of it and keep in going all over. Imagine

> sitting at home with your family and looking at picture after

picture

> of CF people all around the world. And reading their messages,

hearing

> what they have to say, hearing their story. I think it could be

> beautiful, and with good organization and preparation, it could go

on

> and on and on. Imagine the possibilities. We could take it to

> clinics, to have people join in. Each person that has it that

moment

> could get involved in any way that they like, perhaps collecting

some

> pictures and pasting them in yourself. It would give us all a week

or

> two of crafty fun, before mailing the book to its next temporary

home.

>

> Think about it everyone. This would be entirely your call whether

to

> participate, so if its not your thing, you could just take a look

and

> not put in pictures or messages. But for those that want to get

really

> involved it would be a beautiful way to join with the entire world

of

> CF families. I am going to start with my clinic, and my old kids

> clinic. and with permission with the pictures that you guys sent

me.

> Which will be many already, and then send it to one of you to start

the

> chain. The possibilities of this amaze me, I think it could be

magical.

>

> Let me know what you guys think.

>

> Natalia

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

------------------------------------

_____

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Share on other sites

I think this would be great! Let's try it and see what happens.

Tina W., mother of Steph, 18yo wcf

Re: A request.. FOR EVERYONE

Thats a great idea...id love to be a part!Patty H

> Everyone,

>

> can I have come up with this idea, and I want to run it by you

> guys. I want to start a book, like a scrap book of CF kids, teens,

> young adults and adults, and their families all around the world.

A

> book that will contain pictures, messages, whatever you'd like to

place

> in it, that would be sent from home to home where information about

> that person and their family would be added.

> I would start it, and with the permission of the people that sent

me

> pictures, I would place them in the book. Then I would send it to

the

> first person on the list, and on it would go. There is enough

people

> on this list alone to make for an interesting book, but then it

could

> go to others. Hopefully making it back to Canada so that I could

see

> it once in a while. It would join a community of people that is

> relatively small, but that I think needs to stick together. Who

knows,

> it could be published one day. I think it would be amazing.

>

> I would set it up that the person that got the book would email me

and

> I would direct where it would go next. (so personal information

would

> not be in the book and that mailing costs would be minimal/local)

That

> way we could keep track of it and keep in going all over. Imagine

> sitting at home with your family and looking at picture after

picture

> of CF people all around the world. And reading their messages,

hearing

> what they have to say, hearing their story. I think it could be

> beautiful, and with good organization and preparation, it could go

on

> and on and on. Imagine the possibilities. We could take it to

> clinics, to have people join in. Each person that has it that

moment

> could get involved in any way that they like, perhaps collecting

some

> pictures and pasting them in yourself. It would give us all a week

or

> two of crafty fun, before mailing the book to its next temporary

home.

>

> Think about it everyone. This would be entirely your call whether

to

> participate, so if its not your thing, you could just take a look

and

> not put in pictures or messages. But for those that want to get

really

> involved it would be a beautiful way to join with the entire world

of

> CF families. I am going to start with my clinic, and my old kids

> clinic. and with permission with the pictures that you guys sent

me.

> Which will be many already, and then send it to one of you to start

the

> chain. The possibilities of this amaze me, I think it could be

magical.

>

> Let me know what you guys think.

>

> Natalia

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

------------------------------------

_____

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Share on other sites

This is a good idea, except... what about contamination? I hate to

be the paranoid mother, but I don't even let my kids touch the books

in the dentist's waiting room. I just can't see letting my child

with cf handle something that has been passed around to hundreds of

other people with cf. Am I being crazy here? What is the

likelihood of germs being transmitted via scrapbook?

I'm not unusually overprotective, but this seems a little risky to

me. What about putting all the same information on a website?

Everything could be scanned and put into a pdf file so that it could

be printed out just as it was written, or viewed online - with zero

chance of cross-infection. The http://www.cfparents.org website has

space.

Just a thought.

~

mommy of 3, 1 with cf

> That

> > way we could keep track of it and keep in going all over.

Imagine

> > sitting at home with your family and looking at picture after

> picture

> > of CF people all around the world. And reading their messages,

> > and on and on. Imagine the possibilities. We could take it to

> > clinics, to have people join in. Each person that has it that

> moment

> > could get involved in any way that they like, perhaps collecting

> some

> > pictures and pasting them in yourself. It would give us all a

week

> or

> > two of crafty fun, before mailing the book to its next temporary

> home.

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,

I feel the same way, and I just hate being so paranoid... but it's undeniable

that certain things, like mold, aspergillus, loves paper...

But creating a web site scrapbook is a really good alternative.

Kim

> > That

> > > way we could keep track of it and keep in going all over.

> Imagine

> > > sitting at home with your family and looking at picture after

> > picture

> > > of CF people all around the world. And reading their messages,

>

> > > and on and on. Imagine the possibilities. We could take it to

> > > clinics, to have people join in. Each person that has it that

> > moment

> > > could get involved in any way that they like, perhaps collecting

> > some

> > > pictures and pasting them in yourself. It would give us all a

> week

> > or

> > > two of crafty fun, before mailing the book to its next temporary

> > home.

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Share on other sites

I really like this idea also but I also have questions about contamination.

I like 's idea about everyone putting their information on the

internet or something like that, although I am so not smart enough to know how

to set

this up. Anyway, if this idea gets going, please include us!!!!!!!

Sue Pettit of Tupelo, Mississippi

mom to (17 wocf) driving and being the most responsible 17 yo I have

ever seen, (13 wocf) playing baseball, football, band, and whatever

else he can get into, and (12 wcf) into all sports, enjoying lots of

friends, running full speed and doing all she can---diagnosed at 8 days of age

at

LeBonheur Childrens Medical Center in Memphis, Tennessee, now seeing Doctors

Lyrene and Makris (and lots of other wonderful folks, of course) at UAB

Children's Hospital in Birmingham, Alabama

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Natalia - I think its wonderful!!! Did you get the pix I sent you? That

postage thing threw me!

Rosemary in NY with 3 children (13, 11 and 7)

with CF. I have a dog named TOBI and have

coined the phrase " BREATHE DAMMIT "

my new favorite quote is

Any idiot can face a crisis -

it's day to day living that wears you out.

Anton Chekhov

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Natalia,

I think that this sounds like a great idea. You can add a picture of

Abby that I sent to you. Everyone will need to take good care of the

book and be sure to pass it on.

Gale

> Everyone,

>

> can I have come up with this idea, and I want to run it by you

> guys. I want to start a book, like a scrap book of CF kids, teens,

> young adults and adults, and their families all around the world.

A

> book that will contain pictures, messages, whatever you'd like to

place

> in it, that would be sent from home to home where information about

> that person and their family would be added.

> I would start it, and with the permission of the people that sent

me

> pictures, I would place them in the book. Then I would send it to

the

> first person on the list, and on it would go. There is enough

people

> on this list alone to make for an interesting book, but then it

could

> go to others. Hopefully making it back to Canada so that I could

see

> it once in a while. It would join a community of people that is

> relatively small, but that I think needs to stick together. Who

knows,

> it could be published one day. I think it would be amazing.

>

> I would set it up that the person that got the book would email me

and

> I would direct where it would go next. (so personal information

would

> not be in the book and that mailing costs would be minimal/local)

That

> way we could keep track of it and keep in going all over. Imagine

> sitting at home with your family and looking at picture after

picture

> of CF people all around the world. And reading their messages,

hearing

> what they have to say, hearing their story. I think it could be

> beautiful, and with good organization and preparation, it could go

on

> and on and on. Imagine the possibilities. We could take it to

> clinics, to have people join in. Each person that has it that

moment

> could get involved in any way that they like, perhaps collecting

some

> pictures and pasting them in yourself. It would give us all a week

or

> two of crafty fun, before mailing the book to its next temporary

home.

>

> Think about it everyone. This would be entirely your call whether

to

> participate, so if its not your thing, you could just take a look

and

> not put in pictures or messages. But for those that want to get

really

> involved it would be a beautiful way to join with the entire world

of

> CF families. I am going to start with my clinic, and my old kids

> clinic. and with permission with the pictures that you guys sent

me.

> Which will be many already, and then send it to one of you to start

the

> chain. The possibilities of this amaze me, I think it could be

magical.

>

> Let me know what you guys think.

>

> Natalia

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After viewing your posts i wondered about books in cf dr rooms, i

always let ty plays with those...they might be contaminated too i

guees.Never even thought of that.

Patty

> > That

> > > way we could keep track of it and keep in going all over.

> Imagine

> > > sitting at home with your family and looking at picture after

> > picture

> > > of CF people all around the world. And reading their messages,

>

> > > and on and on. Imagine the possibilities. We could take it to

> > > clinics, to have people join in. Each person that has it that

> > moment

> > > could get involved in any way that they like, perhaps

collecting

> > some

> > > pictures and pasting them in yourself. It would give us all a

> week

> > or

> > > two of crafty fun, before mailing the book to its next

temporary

> > home.

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Hmmmm, gee lets see, that is a tough question... " would we want to be

invovled in something like that " ? Well of course!!!!Natalia, I can

literally feel the excitement oozing onto your keyboard. As far as

cross-contamination, well if the scrapbook pages are put into

plastic sleeves and the album itself is plastic coated so one can

use a lysol wipe and wipe the pages and book off.....perhaps this

would help calm the fears of some? My concern is trusting the pages

to the postal service. What a shame it would be to see something

happen after all the work was put into it. I think it's a great idea

and whatever I can do to help, let me know!!

I am glad you got our letter. It sat in my car for awhile....I never

seem to have stamps!

Glad to see you are home!!!

e

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Super idea, count us in for sure!!

Cheryl

A request.. FOR EVERYONE

Everyone,

can I have come up with this idea, and I want to run it by you

guys. I want to start a book, like a scrap book of CF kids, teens,

young adults and adults, and their families all around the world. A

book that will contain pictures, messages, whatever you'd like to place

in it, that would be sent from home to home where information about

that person and their family would be added.

I would start it, and with the permission of the people that sent me

pictures, I would place them in the book. Then I would send it to the

first person on the list, and on it would go. There is enough people

on this list alone to make for an interesting book, but then it could

go to others. Hopefully making it back to Canada so that I could see

it once in a while. It would join a community of people that is

relatively small, but that I think needs to stick together. Who knows,

it could be published one day. I think it would be amazing.

I would set it up that the person that got the book would email me and

I would direct where it would go next. (so personal information would

not be in the book and that mailing costs would be minimal/local) That

way we could keep track of it and keep in going all over. Imagine

sitting at home with your family and looking at picture after picture

of CF people all around the world. And reading their messages, hearing

what they have to say, hearing their story. I think it could be

beautiful, and with good organization and preparation, it could go on

and on and on. Imagine the possibilities. We could take it to

clinics, to have people join in. Each person that has it that moment

could get involved in any way that they like, perhaps collecting some

pictures and pasting them in yourself. It would give us all a week or

two of crafty fun, before mailing the book to its next temporary home.

Think about it everyone. This would be entirely your call whether to

participate, so if its not your thing, you could just take a look and

not put in pictures or messages. But for those that want to get really

involved it would be a beautiful way to join with the entire world of

CF families. I am going to start with my clinic, and my old kids

clinic. and with permission with the pictures that you guys sent me.

Which will be many already, and then send it to one of you to start the

chain. The possibilities of this amaze me, I think it could be magical.

Let me know what you guys think.

Natalia

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

------------------------------------

_____

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It sure sounds like a cute & fun activity ----and friendship

LOVE & Hugs

GRANDMOMBEV

A request.. FOR EVERYONE

Everyone,

can I have come up with this idea, and I want to run it by you

guys. I want to start a book, like a scrap book of CF kids, teens,

young adults and adults, and their families all around the world. A

book that will contain pictures, messages, whatever you'd like to place

in it, that would be sent from home to home where information about

that person and their family would be added.

I would start it, and with the permission of the people that sent me

pictures, I would place them in the book. Then I would send it to the

first person on the list, and on it would go. There is enough people

on this list alone to make for an interesting book, but then it could

go to others. Hopefully making it back to Canada so that I could see

it once in a while. It would join a community of people that is

relatively small, but that I think needs to stick together. Who knows,

it could be published one day. I think it would be amazing.

I would set it up that the person that got the book would email me and

I would direct where it would go next. (so personal information would

not be in the book and that mailing costs would be minimal/local) That

way we could keep track of it and keep in going all over. Imagine

sitting at home with your family and looking at picture after picture

of CF people all around the world. And reading their messages, hearing

what they have to say, hearing their story. I think it could be

beautiful, and with good organization and preparation, it could go on

and on and on. Imagine the possibilities. We could take it to

clinics, to have people join in. Each person that has it that moment

could get involved in any way that they like, perhaps collecting some

pictures and pasting them in yourself. It would give us all a week or

two of crafty fun, before mailing the book to its next temporary home.

Think about it everyone. This would be entirely your call whether to

participate, so if its not your thing, you could just take a look and

not put in pictures or messages. But for those that want to get really

involved it would be a beautiful way to join with the entire world of

CF families. I am going to start with my clinic, and my old kids

clinic. and with permission with the pictures that you guys sent me.

Which will be many already, and then send it to one of you to start the

chain. The possibilities of this amaze me, I think it could be magical.

Let me know what you guys think.

Natalia

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

------------------------------------

_____

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Fantastic idea. We would love to participate. Email poltman@....

Thanks

Lesley & Dave

Mom & dad to Lynn 10.5 no CF and Leanne 5.5 w/CF

A request.. FOR EVERYONE

> Everyone,

>

> can I have come up with this idea, and I want to run it by you

> guys. I want to start a book, like a scrap book of CF kids, teens,

> young adults and adults, and their families all around the world. A

> book that will contain pictures, messages, whatever you'd like to place

> in it, that would be sent from home to home where information about

> that person and their family would be added.

> I would start it, and with the permission of the people that sent me

> pictures, I would place them in the book. Then I would send it to the

> first person on the list, and on it would go. There is enough people

> on this list alone to make for an interesting book, but then it could

> go to others. Hopefully making it back to Canada so that I could see

> it once in a while. It would join a community of people that is

> relatively small, but that I think needs to stick together. Who knows,

> it could be published one day. I think it would be amazing.

>

> I would set it up that the person that got the book would email me and

> I would direct where it would go next. (so personal information would

> not be in the book and that mailing costs would be minimal/local) That

> way we could keep track of it and keep in going all over. Imagine

> sitting at home with your family and looking at picture after picture

> of CF people all around the world. And reading their messages, hearing

> what they have to say, hearing their story. I think it could be

> beautiful, and with good organization and preparation, it could go on

> and on and on. Imagine the possibilities. We could take it to

> clinics, to have people join in. Each person that has it that moment

> could get involved in any way that they like, perhaps collecting some

> pictures and pasting them in yourself. It would give us all a week or

> two of crafty fun, before mailing the book to its next temporary home.

>

> Think about it everyone. This would be entirely your call whether to

> participate, so if its not your thing, you could just take a look and

> not put in pictures or messages. But for those that want to get really

> involved it would be a beautiful way to join with the entire world of

> CF families. I am going to start with my clinic, and my old kids

> clinic. and with permission with the pictures that you guys sent me.

> Which will be many already, and then send it to one of you to start the

> chain. The possibilities of this amaze me, I think it could be magical.

>

> Let me know what you guys think.

>

> Natalia

>

>

> -------------------------------------------

> The opinions and information exchanged on this list should IN NO WAY

> be construed as medical advice.

>

> PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

>

> ------------------------------------

>

>

>

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I think it's a great idea but I have a suggestion.

The idea is to create another group, called CF Profiles, where we can

all post our little chapter into it. As a matter of fact, MSN can be

great for that, since you can have specific categories for each

person - i.e., you can reply to your own segment without having other

people putting information into that piece.

That would make it cheap (free), available to everyone, and no

worries for germs or whatever.

I have done it for my betta clubs (Betta Breeders Profiles) and find

it a great idea.

> Everyone,

>

> can I have come up with this idea, and I want to run it by you

> guys. I want to start a book, like a scrap book of CF kids, teens,

> young adults and adults, and their families all around the world.

A

> book that will contain pictures, messages, whatever you'd like to

place

> in it, that would be sent from home to home where information about

> that person and their family would be added.

> I would start it, and with the permission of the people that sent

me

> pictures, I would place them in the book. Then I would send it to

the

> first person on the list, and on it would go. There is enough

people

> on this list alone to make for an interesting book, but then it

could

> go to others. Hopefully making it back to Canada so that I could

see

> it once in a while. It would join a community of people that is

> relatively small, but that I think needs to stick together. Who

knows,

> it could be published one day. I think it would be amazing.

>

> I would set it up that the person that got the book would email me

and

> I would direct where it would go next. (so personal information

would

> not be in the book and that mailing costs would be minimal/local)

That

> way we could keep track of it and keep in going all over. Imagine

> sitting at home with your family and looking at picture after

picture

> of CF people all around the world. And reading their messages,

hearing

> what they have to say, hearing their story. I think it could be

> beautiful, and with good organization and preparation, it could go

on

> and on and on. Imagine the possibilities. We could take it to

> clinics, to have people join in. Each person that has it that

moment

> could get involved in any way that they like, perhaps collecting

some

> pictures and pasting them in yourself. It would give us all a week

or

> two of crafty fun, before mailing the book to its next temporary

home.

>

> Think about it everyone. This would be entirely your call whether

to

> participate, so if its not your thing, you could just take a look

and

> not put in pictures or messages. But for those that want to get

really

> involved it would be a beautiful way to join with the entire world

of

> CF families. I am going to start with my clinic, and my old kids

> clinic. and with permission with the pictures that you guys sent

me.

> Which will be many already, and then send it to one of you to start

the

> chain. The possibilities of this amaze me, I think it could be

magical.

>

> Let me know what you guys think.

>

> Natalia

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e: When I was younger, cameras hadn't been invented. Rembrandt

made a brass etching of me, but he decided to melt it down. Hal

Re: A request.. FOR EVERYONE

Perhaps we could get n and Hal to send in some picture of when

they were younger and [ictures of them today!

e

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

------------------------------------

_____

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Share on other sites

Sounds like a good one to me! n Rojas

A request.. FOR EVERYONE

Everyone,

can I have come up with this idea, and I want to run it by you

guys. I want to start a book, like a scrap book of CF kids, teens,

young adults and adults, and their families all around the world. A

book that will contain pictures, messages, whatever you'd like to place

in it, that would be sent from home to home where information about

that person and their family would be added.

I would start it, and with the permission of the people that sent me

pictures, I would place them in the book. Then I would send it to the

first person on the list, and on it would go. There is enough people

on this list alone to make for an interesting book, but then it could

go to others. Hopefully making it back to Canada so that I could see

it once in a while. It would join a community of people that is

relatively small, but that I think needs to stick together. Who knows,

it could be published one day. I think it would be amazing.

I would set it up that the person that got the book would email me and

I would direct where it would go next. (so personal information would

not be in the book and that mailing costs would be minimal/local) That

way we could keep track of it and keep in going all over. Imagine

sitting at home with your family and looking at picture after picture

of CF people all around the world. And reading their messages, hearing

what they have to say, hearing their story. I think it could be

beautiful, and with good organization and preparation, it could go on

and on and on. Imagine the possibilities. We could take it to

clinics, to have people join in. Each person that has it that moment

could get involved in any way that they like, perhaps collecting some

pictures and pasting them in yourself. It would give us all a week or

two of crafty fun, before mailing the book to its next temporary home.

Think about it everyone. This would be entirely your call whether to

participate, so if its not your thing, you could just take a look and

not put in pictures or messages. But for those that want to get really

involved it would be a beautiful way to join with the entire world of

CF families. I am going to start with my clinic, and my old kids

clinic. and with permission with the pictures that you guys sent me.

Which will be many already, and then send it to one of you to start the

chain. The possibilities of this amaze me, I think it could be magical.

Let me know what you guys think.

Natalia

-------------------------------------------

The opinions and information exchanged on this list should IN NO WAY

be construed as medical advice.

PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

TREATMENTS.

------------------------------------

_____

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